Global Variome shared LOVD
OCA2 (oculocutaneous albinism II)
LOVD v.3.0 Build 30b [
Current LOVD status
]
Register as submitter
|
Log in
Curator:
William (Bill) Oetting
View all genes
View OCA2 gene homepage
View graphs about the OCA2 gene database
Create a new gene entry
View all transcripts
View all transcripts of gene OCA2
Create a new transcript information entry
View all variants
View all variants affecting transcripts
View unique variants in gene OCA2
View all variants in gene OCA2
Full data view for gene OCA2
Create a new data submission
View active genomic custom columns
Enable more genomic custom columns
View all individuals
View all individuals with variants in gene OCA2
Create a new data submission
View active custom columns
Enable more custom columns
View all diseases
View all diseases associated with gene OCA2
Create a new disease information entry
View available phenotype columns
View all screenings
View all screenings for gene OCA2
Create a new data submission
View active custom columns
Enable more custom columns
Submit new data
All screenings for gene OCA2
Legend
Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.
Template
: Template(s) used to detect the sequence variant; DNA (genomic DNA), RNA (cDNA) or protein
All options:
DNA
RNA = RNA (cDNA)
protein
? = unknown
Technique
: technique(s) used to identify the sequence variant.
All options:
? = unknown
ARMS = amplification refractory mutation system
arrayCGH = array for Comparative Genomic Hybridisation
arrayMET = array for methylation analysis
arraySEQ = array for resequencing
arraySNP = array for SNP typing
arrayCNV = array for Copy Number Variation (SNP and CNV probes)
ASO = allele-specific oligo hybridisation
BESS = Base Excision Sequence Scanning
CMC = Chemical Mismatch Cleavage
COBRA = Combined Bisulfite Restriction Analysis
CSCE = Conformation Sensitive Capillary Electrophoresis
CSGE = Conformation Sensitive Gel Electrophoresis
ddF = dideoxy Fingerprinting
DGGE = Denaturing-Gradient Gel-Electrophoresis
DHPLC = Denaturing High-Performance Liquid Chromatography
DOVAM = Detection Of Virtually All Mutations (SSCA variant)
DSCA = Double-Strand DNA Conformation Analysis
DSDI = Detection Small Deletions and Insertions
EMC = Enzymatic Mismatch Cleavage
expr = expression analysis
FISH = Fluorescent In-Situ Hybridisation
FISHf = fiberFISH
HD = HeteroDuplex analysis
HPLC = High-Performance Liquid Chromatography
IEF = IsoElectric Focussing
IHC = Immuno-Histo-Chemistry
Invader = Invader assay
MAPH = Multiplex Amplifiable Probe Hybridisation
MAQ = Multiplex Amplicon Quantification
MCA = Melting Curve Analysis, high-resolution (HRMA)
microscope = microscopic analysis (karyotype)
microsat = microsatellite genotyping
minigene = expression minigene construct
MIP = Molecular Inversion Probe amplification
MIPsm = single molecule Molecular Inversion Probe amplification
MLPA = Multiplex Ligation-dependent Probe Amplification
MLPA-ms = Multiplex Ligation-dependent Probe Amplification, methylation specific
MS = mass spectrometry
Northern = Northern blotting
NUC = nuclease digestion (RNAseT1, S1)
OM = optical mapping
PAGE = Poly-Acrylamide Gel-Electrophoresis
PCR = Polymerase Chain Reaction
PCRdd = PCR, digital droplet
PCRdig = PCR + restriction enzyme digestion
PCRh = PCR, haloplex
PCRlr = PCR, long-range
PCRm = PCR, multiplex
PCRms = PCR, methylation sensitive
PCRq = PCR, quantitative (qPCR)
PCRrp = PCR, repeat-primed (RP-PCR)
PCRsqd = PCR, semi-quantitative duplex
PE = primer extension (APEX, SNaPshot)
PEms = primer extension, methylation-sensitive single-nucleotide
PFGE = Pulsed-Field Gel-Electrophoresis (+Southern)
PTT = Protein Truncation Test
RFLP = Restriction Fragment Length Polymorphisms
RT-PCR = Reverse Transcription and PCR
RT-PCRq = Reverse Transcription and PCR, quantitative
SBE = Single Base Extension
SEQ = SEQuencing (Sanger)
SEQb = bisulfite SEQuencing
SEQp = pyroSequencing
SEQms = sequencing, methylation specific
SEQ-ON = next-generation sequencing - Oxford Nanopore
SEQ-NG = next-generation sequencing
SEQ-NG-RNA = next-generation sequencing RNA
SEQ-NG-H = next-generation sequencing - Helicos
SEQ-NG-I = next-generation sequencing - Illumina/Solexa
SEQ-NG-IT = next-generation sequencing - Ion Torrent
SEQ-NG-R = next-generation sequencing - Roche/454
SEQ-NG-S = next-generation sequencing - SOLiD
SEQ-PB = next-generation sequencing - Pacific Biosciences
SNPlex = SNPlex
Southern = Southern blotting
SSCA = Single-Strand DNA Conformation polymorphism Analysis (SSCP)
SSCAf = fluorescent SSCA (SSCP)
STR = Short Tandem Repeat
TaqMan = TaqMan assay
Western = Western blotting
- = not applicable
Tissue
: tissue type used for analysis
Remarks
: remarks regarding the screening like WGS (whole genome sequencing), WES (whole exome sequencing, gene panel (incl. a list of genes analysed), etc.
How to query this table
All list views have search fields which can be used to search data. You can search for a complete word or you can search for a part of a search term. If you enclose two or more words in double quotes, LOVD will search for the combination of those words only exactly in the order you specify. Note that search terms are case-insensitive and that wildcards such as * are treated as normal text! For all options, like "and", "or", and "not" searches, or searching for prefixes or suffixes, see the table below.
Operator
Column type
Example
Matches
Text
Arg
all entries containing 'Arg'
space
Text
Arg Ser
all entries containing 'Arg' and 'Ser'
|
Text
Arg|Ser
all entries containing 'Arg' or 'Ser'
!
Text
!fs
all entries not containing 'fs'
^
Text
^p.(Arg
all entries beginning with 'p.(Arg'
$
Text
Ser)$
all entries ending with 'Ser)'
=""
Text
=""
all entries with this field empty
=""
Text
="p.0"
all entries exactly matching 'p.0'
!=""
Text
!=""
all entries with this field not empty
!=""
Text
!="p.0"
all entries not exactly matching 'p.0?'
combination
Text
*|Ter !fs
all entries containing '*' or 'Ter' but not containing 'fs'
Date
2020
all entries matching the year 2020
|
Date
2020-03|2020-04
all entries matching March or April, 2020
!
Date
!2020-03
all entries not matching March, 2020
<
Date
<2020
all entries before the year 2020
<=
Date
<=2020-06
all entries in or before June, 2020
>
Date
>2020-06
all entries after June, 2020
>=
Date
>=2020-06-15
all entries on or after June 15th, 2020
combination
Date
2019|2020 <2020-03
all entries in 2019 or 2020, and before March, 2020
Numeric
23
all entries exactly matching 23
|
Numeric
23|24
all entries exactly matching 23 or 24
!
Numeric
!23
all entries not exactly matching 23
<
Numeric
<23
all entries lower than 23
<=
Numeric
<=23
all entries lower than, or equal to, 23
>
Numeric
>23
all entries higher than 23
>=
Numeric
>=23
all entries higher than, or equal to, 23
combination
Numeric
>=20 <30 !23
all entries with values from 20 to 29, but not equal to 23
Some more advanced examples:
Example
Matches
Asian
all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc.
Asian !Caucasian
all entries containing 'Asian' but not containing 'Caucasian'
Asian|African !Caucasian
all entries containing 'Asian' or 'African', but not containing 'Caucasian'
"South Asian"
all entries containing 'South Asian', but not containing 'South East Asian'
To sort on a certain column, click on the column header or on the arrows. If that column is already selected to sort on, the sort order will be swapped. The column currently sorted on has a darker blue background color than the other columns. The up and down arrows next to the column name indicate the current sorting direction. When sorting on any field other than the default, LOVD will sort secondarily on the default sort column.
40 entries on 1 page. Showing entries 1 - 40.
10 per page
25 per page
50 per page
100 per page
Legend
How to query
Screening ID
Individual ID
Template
Technique
Tissue
Remarks
Variants found
Owner
0000074683
00074519
DNA
SEQ
-
-
2
Pieter Klap
0000074684
00074520
DNA
SEQ
-
-
2
Pieter Klap
0000074712
00074549
DNA
SEQ
-
-
2
Pieter Klap
0000074716
00074553
DNA
SEQ
-
-
3
Pieter Klap
0000074717
00074554
DNA
SEQ
-
-
1
Pieter Klap
0000074718
00074555
DNA
SEQ
-
-
1
Pieter Klap
0000074719
00074556
DNA
SEQ
-
-
1
Pieter Klap
0000074721
00074557
DNA
SEQ
-
-
1
Pieter Klap
0000074722
00074559
DNA
SEQ
-
-
1
Pieter Klap
0000074728
00074565
DNA
SEQ
-
-
1
Pieter Klap
0000074730
00074567
DNA
SEQ
-
-
2
Pieter Klap
0000101363
00100940
DNA
SEQ
-
-
1
Gemeinschaftspraxis für Humangenetik Dresden
0000132896
00132057
DNA
SEQ
-
-
1
Gemeinschaftspraxis für Humangenetik Dresden
0000309671
00308526
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000309672
00308527
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000329288
00328073
DNA
SEQ-NG
-
WGS
2
LOVD
0000329335
00328120
DNA
SEQ-NG
-
WGS
1
LOVD
0000375139
00373907
DNA
SEQ-NG
-
238-gene panel
2
LOVD
0000383367
00382151
DNA
SEQ-NG
blood
-
1
LOVD
0000383368
00382152
DNA
SEQ-NG
blood
-
1
LOVD
0000386724
00385495
DNA
SEQ-NG
blood
18 genes panel tested
1
LOVD
0000386727
00385498
DNA
SEQ-NG
blood
18 genes panel tested
1
LOVD
0000386730
00385501
DNA
SEQ-NG
blood
18 genes panel tested
1
LOVD
0000386756
00385527
DNA
SEQ-NG
blood
18 genes panel tested
2
LOVD
0000386757
00385528
DNA
SEQ-NG
blood
18 genes panel tested
1
LOVD
0000386766
00385537
DNA
SEQ-NG
blood
18 genes panel tested
1
LOVD
0000386767
00385538
DNA
SEQ-NG
blood
18 genes panel tested
2
LOVD
0000386773
00385544
DNA
SEQ-NG
blood
26 genes panel tested
2
LOVD
0000391568
00390327
DNA
SEQ-NG-I
blood
whole genome sequencing
2
LOVD
0000392039
00390798
DNA
arraySEQ
Blood
-
2
LOVD
0000392624
00391382
DNA
SEQ-NG
-
retrospective case note review, targeted gene panel testing
1
LOVD
0000438107
00436624
DNA
SEQ-NG
BLOOD
-
1
Sudha Kohli, Renu Saxena, Ratna Puri, I.C. Verma
0000466964
00465316
DNA
SEQ
blood
-
1
Gemeinschaftspraxis für Humangenetik Dresden
0000467035
00465386
DNA
SEQ;MLPA
-
-
2
Johan den Dunnen
0000467036
00465387
DNA
SEQ;MLPA
-
-
1
Johan den Dunnen
0000467037
00465388
DNA
SEQ;MLPA
-
-
2
Johan den Dunnen
0000467038
00465389
DNA
SEQ;MLPA
-
-
2
Johan den Dunnen
0000467039
00465390
DNA
SEQ;MLPA
-
-
1
Johan den Dunnen
0000467040
00465391
DNA
SEQ;MLPA
-
-
1
Johan den Dunnen
0000467041
00465392
DNA
SEQ;MLPA
-
-
1
Johan den Dunnen
10 per page
25 per page
50 per page
100 per page
Legend
How to query
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our
APIs
to retrieve data.
Powered by
LOVD v.3.0
Build 30b
LOVD software ©2004-2024
Leiden University Medical Center
Database contents © by their respective submitters and curators